Canonical Allele Identifier: PA2825342595
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 585761
ClinVar RCV Id: RCV000711397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Ile415Met
CA4904950
NM_001026213.1:c.1245A>G